Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display Forming a New Life: Conception, Heredity, and Environment.

Slides:



Advertisements
Similar presentations
Human Genetic Disorders
Advertisements

Honors Biology Genetic Disorders.
Sickle Cell Anemia Blood disorder, inherited disease where a person inherits a mutant gene form each parent for the manufacture of hemoglobin. Red blood.
Birth Defects.
KARYOTYPE AND GENETIC DISORDERS
Chapter 12 Patterns of Heredity and Human Genetics
NOTES 24 – Genetic Disorders and Hereditary Diseases
What’s Your Blood Type? A B AB O.
 What’s a “mutagen”?  What does a mutation do to DNA?  If a mutation affects a gene, then what might happen to the protein sequence?
PowerPoint Lecture Outlines to accompany
Chapter 12: Patterns of Heredity & Human Genetics
GENETIC DISORDERS & DISEASES. Types?  Dominant  Recessive  Sex Linked  Chromosomal  Mutagens?
Human Genetics.
Human Genetic disorders
List at least 3 genetic conditions you know of. Why do you think they are genetic conditions?
Beginnings PART 2 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
INHERITED GENETIC DISORDERS
Chapter 24: Patterns of Chromosome Inheritance
Complex Patterns of Inheritance and Meiosis inheritance mistakes.
Genetic Disorders and Birth Defects. Cleft lip/pallet Affects: anyone, more common in asians and native americans When appears: birth Method of inheritance:
IN Today we will be studying several common genetic disorders inherited by humans. How do you think a FAMILY is impacted when a child in the family is.
1. Somatic cells in humans have __________ chromosomes. A. 23 B. 46 C
Mendelian Genetics Chapter 11 Part 2 pp ,
Mutations and other genetic issues
Genetic Crosses. Genetics “study of genes and heredity” “study of genes and heredity” Gene – segment of DNA that codes for a Gene – segment of DNA that.
Ch 20 Lesson 2 From Generation to Generation. Things to do before we start class…  Take out Prenatal Development Worksheet.
Chapter 4, Section 2 Human Genetic Disorders
Chapter 12.  Humans have 46 chromosomes  44 are autosomes  22 pairs of homologous chromosomes  2 are sex chromosomes: X and Y  Females have two X.
Influences on Birth Defects. FACTS About 150,000 babies are born each year with birth defects. The parents of one out of every 28 babies receive the frightening.
SEX DETERMINATION The sex of an individual is determined by the sex chromosomes contributed to the zygote by the sperm and the egg.
PowerPoint Lecture Outlines to accompany
Heredity, Environment, and the Beginnings of Human Life The Life Span Human Development for Healthcare Professionals, Chapter 2.
Jeopardy Key TermsHereditary EnvironmentBirth Defects Wild Card Q $100 Q $200 Q $300 Q $400 Q $500 Q $100 Q $200 Q $300 Q $400 Q $500 Final Jeopardy.
Important Genetic Disorders Bio. Definitions ► Autosomes- any chromosome that is not a sex chromosome. Not the “X” or “Y” ► Sex-linked- genes located.
Human Genetic Disorders
ABO Blood Groups and Genetic Disorders
HUMAN GENETICS. Objectives 2. Discuss the relationships among chromosomes, genes, and DNA. 2.8 Examine incomplete dominance, alleles, sex determination,
Human Inheritance. Review – What is Heredity? Heredity is the passing of traits from parents to offspring Genes are passed from parents to offspring (**Remember.
Genetics. Color Blindness w Occurs more frequently in men w sex-linked (X) w affects light receptors in the eye red/green complete.
Muscular Dystrophy. The Defect Muscular dystrophy is a group of inherited disorders that involve muscle weakness and loss of muscle tissue, which get.
Human Genes & Chromosomes. Human Genetic Disorders Nondisjunction is a cause of some human genetic disorders –In nondisjunction, the members of a chromosome.
Chapter 15: Human Genetics
Human Genetic Disorders Biology. Mutations Sometimes genes are damaged or copied incorrectly. A change in a gene is called a mutation. Mutations are a.
Genetics. Color Blindness w Occurs more frequently in men w sex-linked (X) w affects light receptors in the eye red/green complete.
Human Genetics.
End Show Slide 1 of 43 Copyright Pearson Prentice Hall 14–1 Human Heredity 14-1 Human Heredity.
Pedigree Used to show how a particular trait is passed from one generation to the next in a family.
 Studying humans requires alternative methods.  Human geneticists use.  Human are – Deduce the genotypes and phenotypes of individuals in.
Name 2 Genetic Diseases. Copyright Pearson Prentice Hall.
Human Genome. Karyotype – a picture of a cell’s chromosomes group in homologous pairs Humans have 46 chromosomes Two of these are sex chromosomes (XX.
Genetic Disorders What is a Genetic Disorder? Caused by abnormalities in an individual’s genetic material (the DNA, or the genome). There are four different.
Generation to Generation Chromosomes: Tiny structures with in the nuclei of cells that carry information about heredity traits. ~Cells in the body contain.
Heredity and Genetics. Every person inherits traits such as hair and eye color as well as the shape of their earlobes from their parents. Inherited traits.
Genetics Gregor Mendel– the “father” of genetics A genetic characteristic generally has two (or more) possible varieties– known as traits. Ex. Plant height:
Diseases and karyotypes
Heredity and Genetics (2:39) Click here to launch video Click here to download print activity.
Human Genetic Disorders Notes. What causes genetic disorders? Mutations, or changes in a person’s DNA.
GENETICS AND GENETICALLY LINKED DISEASES Chapter 22.
Chapter 14 Human Heredity. Human Chromosomes A picture of chromosomes arranged in this way (previous page) is know as a karyotype. This karyotype is.
SEX DETERMINATION The sex of an individual is determined by the sex chromosomes contributed to the zygote by the sperm and the egg.
Chapter 12 Patterns of Heredity And Human Genetics.
Warm Up Things that are changed in an experiment are called the ___________________.
Section 7-1 “Human genetics”
INHERITED GENETIC DISORDERS
Different mode and types of inheritance
Copyright Pearson Prentice Hall
Chapter 12.2-When Heredity Follows Different Rules
Patterns of inheritance
Inheritance of Genetic Traits
Presentation transcript:

Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display Forming a New Life: Conception, Heredity, and Environment Chapter 2

Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display Guideposts for Study 1.How are birth defects and disorders transmitted?

Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display Mechanisms of Heredity Genetic and Chromosomal Abnormalities Some defects are due to abnormalities in genes or chromosomes, which may result from ________________ Many disorders arise when an inherited predisposition interacts with an environmental factor, either before or after birth

Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display Mechanisms of Heredity Genetic ____________________ A chart called a _______________ can show chromosomal abnormalities and can indicate whether a person who appears normal might transmit genetic defects to a child

Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display Should genetic counseling be compulsory before marriage?

Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display Defects Transmitted by Dominant Inheritance ____________ genes are usually dominant When one parent has a dominant abnormal gene and one recessive normal gene and the other parent has two recessive genes, each of their children has a 50:50 chance of inheriting Example – ___________________disease

Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display Defects Transmitted by Recessive Inheritance _____________ defects are expressed only if a child receives the same recessive gene from each biological parent Defects transmitted by recessive inheritance are more likely to be __________ at an early age Example – _________________

Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display Cystic fibrosis Body makes too much _______________ Children do not grow normally Usually do not live beyond age ________ Most common inherited lethal defect among ________________ people

Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display Duchenne’s Muscular Dystrophy __________disease usually found in males Marked by muscle weakness, minor mental retardation Respiratory failure and death usually occur in ______________ adulthood

Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display Spina Bifida Incompletely closed spinal canal, resulting in muscle weakness or paralysis and loss of bladder and bowel control Often accompanied by ________________ which is an accumulation of spinal fluid in the brain (may lead to mental retardation)

Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display Sickle-cell anemia Deformed, fragile ________ blood cells that can clog the blood vessels – deprives the body of _____________ Symptoms include severe pain, stunted growth, frequent infections, leg ulcers, gallstones, susceptibility to pneumonia, and stroke Found among ______________ descent

Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display Tay-Sachs Disease Degenerative disease of the brain and nerve cells Results in death before age ______ Found among people of European ___________ descent

Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display Defects Transmitted by Sex-Linked Inheritance Sex-linked inheritance: Pattern of inheritance in which certain characteristics carried on the X chromosome inherited from the mother are transmitted differently to her male and female offspring.

Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display Chromosomal Abnormalities Down syndrome: Chromosomal disorder characterized by moderate to severe mental retardation and a downward sloping skin fold at the inner corners of the eyes. Also called _________________________

Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display Sex Chromosome Abnormalities Fragile X Minor-to-severe mental retardation Symptoms more severe in ______________ Include delayed speech and motor development, speech impairments, hyperactivity The ___________ common inherited form of mental retardation